反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A water cooled stirred suspension of 13.41 g (0.05 mol) of 6,11-dihydro-11-oxodibenz[b,e]oxepin-2-yl acetic acid, 50 ml of sieve-dried methylene chloride and three drops of dimethylformamide was treated for a few minutes with 6.54 g (0.055 mol) of thionyl chloride. After total addition the suspension was stirred 15 minutes with cooling and was then intermittently warmed until the evolution of HCl ceased. A stirred ice water chilled solution of 13.37 g (0.15 mol) of 2-amino-2-methyl-1-propanol and 50 ml of sieve-dried methylene chloride was treated dropwise over 0.5 hour with the acid chloride solution. After total addition the resultant suspension was stirred with cooling for 20 minutes and was then stirred 1.5 hours at ambient temperature. The suspension was vacuum filtered and the filtrate was washed with 100 ml each of 5% HCl, water, and 5% Na2CO3. The organic phase was dried by extracting with 500 ml of saturated NaCl solution and then over anhydrous Na2SO4. The resultant mixture was filtered and the filtrate was concentrated to an oil which was dried by azeotropic distillation of absolute ethanol to afford 14.3 g (84.3%) of a crude product. Two recrystallizations from benzene and a final recrystallization from isopropanol afforded 7.0 g (41.2%) of crystals of 6,11-dihydro-N-(1-hydroxy-2-methyl-2-propyl)-11-oxodibenz[b,e]oxepin-2-yl acetamide m.p. 132°-134° C.
WORKUP
后处理
- additionAfter total addition the suspension
- stirringwas stirred 15 minutes
- temperaturewith cooling
- stirringwas stirred
- temperaturewith cooling for 20 minutes
- stirringwas then stirred 1.5 hours at ambient temperature
- filtrationfiltered
- washthe filtrate was washed with 100 ml each of 5% HCl, water, and 5% Na2CO3
- customThe organic phase was dried
- extractionby extracting with 500 ml of saturated NaCl solution
- filtrationThe resultant mixture was filtered
- concentrationthe filtrate was concentrated to an oil which
- dry with materialwas dried by azeotropic distillation of absolute ethanol
- customto afford 14.3 g (84.3%) of a crude product
- customTwo recrystallizations from benzene
- customa final recrystallization from isopropanol